FDA Adverse Event Injury Summary report: N

KANGAROO NASOGASTRIC TUBE

MDR report key: 3522887 · Received November 25, 2013

Report

Report Number
3522887
Event Type
Injury
Date Received
November 25, 2013
Date of Event
October 24, 2013
Report Date
November 25, 2013
Manufacturer
COVIDIEN
Product Code
KNT
Adverse Event
Yes
Product Problem
Yes
Report Source
User Facility report
Reporter Location
NY, US
Reporter Occupation
RISK MANAGER

Narratives

Description of Event or Problem · 1

NG TUBE INSERTED TO ALLOW FOR FEEDING. CONFIRMING CHEST X-RAY INDICATED NGT IN THE RIGHT TRACHEOBRONCHIAL TREE TO THE RIGHT PLEURAL SURFACE. IT ENDED POSSIBLY BELOW THE DIAPHRAGM IN A DEEP LATERAL PLEURAL SULCUS. NGT REPLACED AND CONFIRMING CHEST X-RAY SHOWED NGT IN STOMACH SMALL RIGHT PNEUMOTHORAX SUSPECTED. PT STARTED ON REBREATHING MASK. X-RAY (B)(6) 2013 SHOWED RIGHT APICAL PNEUMOTHORAX. CHEST X-RAY (B)(6) 2013 SHOWED PNEUMOTHORAX RESOLVED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
612679 KANGAROO NASOGASTRIC TUBE NONE KNT COVIDIEN 8884-720858 8FR 43"

Patients

Seq Age Sex Outcome Treatment
1 77 YR Required Intervention